Salivary gland-type lung tumor: An update

被引:6
|
作者
Gibault, Laure [1 ]
Badoual, Cecile [1 ,2 ]
机构
[1] Hop Europeen Georges Pompidou, AP HP, Serv Anat Pathol, 20 Rue Leblanc, F-75015 Paris, France
[2] PARCC, Fac Paris Descartes, INSERM, U970,Equipe 10, 56 Rue Leblanc, F-75015 Paris, France
关键词
Pulmonary salivary gland-type carcinoma; Mucoepidermoid carcinoma; Adenoid cystic carcinoma; Pleomorphic adenoma; Mucous gland adenoma; MUCOEPIDERMOID CARCINOMA; PLEOMORPHIC ADENOMA; FEATURES; BRONCHUS; EGFR;
D O I
10.1016/j.annpat.2015.11.003
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
"Salivary gland-type" tumors arising from the bronchi and lung are rare but not exceptional entities. They are mostly represented by malignant entities such as cystic adenoid carcinoma, mucoepidermoid carcinoma and epithelial/myoepithelial carcinoma. Benign tumors are rare, mainly encompassing pleomorphic adenomas, which are to differentiate from mucous gland adenomas, another entity arising specifically from the peri-bronchial glands. These tumours develop in the proximal bronchi and are not associated with smoke abuse. Their main treatment is surgery. It is important to differentiate them from other broncho-pulmonary tumours as they do not share the same prognosis and therapeutic. This article will review the WHO 2015 classification of these tumours as well as recent updates from the literature to help define diagnosis criteria for these uncommon entities. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
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